Case Report
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45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu

Year 2019, Volume: 3 Issue: 1, 31 - 33, 28.04.2019

Abstract

Turner sendromu, önemli bir
infertilite nedenidir ancak
mozaik veya X
delesyonu taşıyan hastalarda eğer puberteye spontan olarak girilmişse gebelik
gerçekleşebilmektedir.
Unikornuat
uterus ise gebelik kaybına yol açabilen ve çok nadir rastlanılan bir uterus anomalisidir.
Şu anki o
lgu, nadir görülmesi ve Turner sendromlu
hastalarda gebelik kayıplarının bir nedenin ortaya konması gibi yönleriyle
literatüre katkı sağlamak amacıyla sunulmuştur.

References

  • 1. Stochholm K, Juul S, Juel K, Naeraa RW, Gravholt CH. Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome. J Clin Endocrinol Metab. 2006; 91:3897–3902. [PubMed: 16849410] https://www.ncbi.nlm.nih.gov/pubmed/16849410
  • 2. Nussbaum, R.L.,Mclnnes, R.R., Willard, H.F.: Thompson&Thompson Genetics in Medicine, 6th Ed, Saunders, Phledelphia, 2005: 174-176. https://www.ncbi.nlm.nih.gov/nlmcatalog/101653590
  • 3. Verschraegen-Spae MR, Depypere H, Speleman F, Dhondt M, De Paepe. Familial Turner syndrome. Clin Genet 1992;41(4): 218-20. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-0004.1992.tb03666.x
  • 4. Lemli L, Smith DW. The XO syndrome: A study of the differentiated phenotype in 25 patients. J Pediatr 1963; 63(Oct):577-88. https://www.sciencedirect.com/science/article/pii/S0022347663803686?via%3Dihub
  • 5. Morgan T.;Turner Syndrome: Diagnosis and Management. Am Fam Physician. 2007; 76(3):405-417.
  • 6. Al Sheikh M, Dunger DB, Conway GS, Wass JAH. Turner’s syndrome in Adulthood Endocr Rev 2002; 23:120–140.
  • 7. Speroff L, Glass RH, Kase NG. Clinical Gynecologic Endocrinology and Infertility. 6th ed. Baltimore: Lippincott Williams & Wilkins; 1999: 123-58.

A case with 45,X[75]/46,Xdel(X)(p11.2)[25] unicornuate uterus

Year 2019, Volume: 3 Issue: 1, 31 - 33, 28.04.2019

Abstract

Turner syndrome is a major cause of infertility, but
pregnancy can occur in cases with the mosaic or X-defect who spontaneously enter
puberty. Unicornuate uterus is the rarest uterine anomaly that can lead to loss
of pregnancy. The current case is presented because she is rare and a cause of
pregnancy loss in patients with Turner's syndrome for the contribution to the
literature.

References

  • 1. Stochholm K, Juul S, Juel K, Naeraa RW, Gravholt CH. Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome. J Clin Endocrinol Metab. 2006; 91:3897–3902. [PubMed: 16849410] https://www.ncbi.nlm.nih.gov/pubmed/16849410
  • 2. Nussbaum, R.L.,Mclnnes, R.R., Willard, H.F.: Thompson&Thompson Genetics in Medicine, 6th Ed, Saunders, Phledelphia, 2005: 174-176. https://www.ncbi.nlm.nih.gov/nlmcatalog/101653590
  • 3. Verschraegen-Spae MR, Depypere H, Speleman F, Dhondt M, De Paepe. Familial Turner syndrome. Clin Genet 1992;41(4): 218-20. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-0004.1992.tb03666.x
  • 4. Lemli L, Smith DW. The XO syndrome: A study of the differentiated phenotype in 25 patients. J Pediatr 1963; 63(Oct):577-88. https://www.sciencedirect.com/science/article/pii/S0022347663803686?via%3Dihub
  • 5. Morgan T.;Turner Syndrome: Diagnosis and Management. Am Fam Physician. 2007; 76(3):405-417.
  • 6. Al Sheikh M, Dunger DB, Conway GS, Wass JAH. Turner’s syndrome in Adulthood Endocr Rev 2002; 23:120–140.
  • 7. Speroff L, Glass RH, Kase NG. Clinical Gynecologic Endocrinology and Infertility. 6th ed. Baltimore: Lippincott Williams & Wilkins; 1999: 123-58.
There are 7 citations in total.

Details

Primary Language Turkish
Subjects Clinical Sciences
Journal Section Case Reports
Authors

Recep Eröz

Mehmet Köksal 0000-0002-2643-5964

Mustafa Doğan

Hüseyin Yüce

Alper Başbuğ

Publication Date April 28, 2019
Published in Issue Year 2019 Volume: 3 Issue: 1

Cite

APA Eröz, R., Köksal, M., Doğan, M., Yüce, H., et al. (2019). 45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu. Ahi Evran Medical Journal, 3(1), 31-33.
AMA Eröz R, Köksal M, Doğan M, Yüce H, Başbuğ A. 45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu. Ahi Evran Med J. April 2019;3(1):31-33.
Chicago Eröz, Recep, Mehmet Köksal, Mustafa Doğan, Hüseyin Yüce, and Alper Başbuğ. “45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine Sahip Unikornuat Uteruslu Olgu”. Ahi Evran Medical Journal 3, no. 1 (April 2019): 31-33.
EndNote Eröz R, Köksal M, Doğan M, Yüce H, Başbuğ A (April 1, 2019) 45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu. Ahi Evran Medical Journal 3 1 31–33.
IEEE R. Eröz, M. Köksal, M. Doğan, H. Yüce, and A. Başbuğ, “45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu”, Ahi Evran Med J, vol. 3, no. 1, pp. 31–33, 2019.
ISNAD Eröz, Recep et al. “45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine Sahip Unikornuat Uteruslu Olgu”. Ahi Evran Medical Journal 3/1 (April 2019), 31-33.
JAMA Eröz R, Köksal M, Doğan M, Yüce H, Başbuğ A. 45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu. Ahi Evran Med J. 2019;3:31–33.
MLA Eröz, Recep et al. “45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine Sahip Unikornuat Uteruslu Olgu”. Ahi Evran Medical Journal, vol. 3, no. 1, 2019, pp. 31-33.
Vancouver Eröz R, Köksal M, Doğan M, Yüce H, Başbuğ A. 45,X[75]/46,Xdel(X)(p11.2)[25] Karyotipine sahip unikornuat uteruslu olgu. Ahi Evran Med J. 2019;3(1):31-3.

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